Intraspecific Diversity of Microbial Anti-Inflammatory Molecule (MAM) from Faecalibacterium prausnitzii

Int J Mol Sci. 2022 Feb 1;23(3):1705. doi: 10.3390/ijms23031705.

Abstract

The commensal bacterium Faecalibacterium prausnitzii has unique anti-inflammatory properties, at least some of which have been attributed to its production of MAM, the Microbial Anti-inflammatory Molecule. Previous phylogenetic studies of F. prausnitzii strains have revealed the existence of various phylogroups. In this work, we address the question of whether MAMs from different phylogroups display distinct anti-inflammatory properties. We first performed wide-scale identification, classification, and phylogenetic analysis of MAM-like proteins encoded in different genomes of F. prausnitzii. When combined with a gene context analysis, this approach distinguished at least 10 distinct clusters of MAMs, providing evidence for functional diversity within this protein. We then selected 11 MAMs from various clusters and evaluated their anti-inflammatory capacities in vitro. A wide range of anti-inflammatory activity was detected. MAM from the M21/2 strain had the highest inhibitory effect (96% inhibition), while MAM from reference strain A2-165 demonstrated only 56% inhibition, and MAM from strain CNCM4541 was almost inactive. These results were confirmed in vivo in murine models of acute and chronic colitis. This study provides insights into the family of MAM proteins and generates clues regarding the choice of F. prausnitzii strains as probiotics for use in targeting chronic inflammatory diseases.

Keywords: Faecalibacterium prausnitzii; microbial anti-inflammatory molecule; probiotic.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / therapeutic use
  • Bacterial Proteins / chemistry
  • Bacterial Proteins / genetics*
  • Bacterial Proteins / therapeutic use
  • Base Sequence
  • Colitis / drug therapy
  • Faecalibacterium prausnitzii / genetics
  • Faecalibacterium prausnitzii / metabolism*
  • Genetic Variation
  • Genome, Bacterial
  • Male
  • Mice
  • Phylogeny*
  • Probiotics / therapeutic use*
  • Sequence Analysis, DNA

Substances

  • Anti-Inflammatory Agents
  • Bacterial Proteins